FDA Adverse Event Injury Summary report: N

OSFERION

MDR report key: 5170545 · Received October 23, 2015

Report

Report Number
3007738819-2015-00017
Event Type
Injury
Date Received
October 23, 2015
Report Date
September 28, 2015
Manufacturer
OLYMPUS TERUMO BIOMATERIALS CORP. MISHIMA FACTORY
Product Code
MQV
PMA / PMN Number
K080065
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

THE DEVICE HISTORY RECORD WAS REVIEWED, AND NO IRREGULARITIES WERE NOTED. MEANWHILE, WE CANNOT RULE OUT THE POSSIBILITY THAT THIS EVENT WAS CAUSED BY EITHER OTHER INTRAOPERATIVE FACTORS OR OTHER FACTORS RELATED TO POSTOPERATIVE MANAGEMENT. BECAUSE THE DEVICE (REFERENCED IN THIS REPORT) WAS NOT RETURNED TO OLYMPUS TERUMO BIOMATERIALS CORP. FOR EVALUATION, THE CAUSE OF THE ADVERSE EVENT HAVE NOT BEEN SPECIFIED. THE OSFERION BONE VOID FILLER PACKAGE INSERT STATES IN THE FOLLOWING SECTION: <ADVERSE EVENTS> INFECTION. FEVER,PAIN,LOCAL SENSATION,RED FLARE,INFLAMMATION. THIS REPORT IS BEING SUBMITTED AS A MEDICAL DEVICE REPORT IS AN ABUNDANCE OF CAUTION.

Description of Event or Problem · 1

CASE) A CASE TREATED WITH HIGH TIBIAL OSTEOTOMY (HTO). AFTER THE TIBIAL OSTEOTOMY, THE RESULTANT BONE DEFECT WAS FILLED WITH A PIECE OF BONE VOID FILLER (HEREAFTER, THIS PRODUCT) TRIMMED CORRESPONDING TO THE SHAPE OF THE BONE DEFECT. THEN THE OSTEOTOMIZED TIBIA WAS FIXED WITH A METAL PLATE AND SCREWS ALL OF WHICH ARE EXCLUSIVELY USED FOR INTERNAL FIXATION. AFTER THE SURGERY, HOWEVER, IT CONFIRMED THE SUSPICION OF SUPERFICIAL INFECTION. CURRENTLY, THE SYMPTOMS SUBSIDED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
702110 OSFERION FILLER, BONE VOID, CALCIUM COMPOUND MQV OLYMPUS TERUMO BIOMATERIALS CORP. MISHIMA FACTORY M15313B619

Patients

Seq Age Sex Outcome Treatment
1 65 YR Hospitalization